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Results: 11

Cited In for PubMed (Select 12915559)

1.

Ectopic DNMT3L triggers assembly of a repressive complex for retroviral silencing in somatic cells.

Kao TH, Liao HF, Wolf D, Tai KY, Chuang CY, Lee HS, Kuo HC, Hata K, Zhang X, Cheng X, Goff SP, Ooi SK, Bestor TH, Lin SP.

J Virol. 2014 Sep;88(18):10680-95. doi: 10.1128/JVI.01176-14. Epub 2014 Jul 2.

2.

Site-specific modulation of brain glucocorticoid receptor and corticotropin-releasing hormone expression using lentiviral vectors.

Laryea G, Arnett MG, Wieczorek L, Muglia LJ.

Mol Cell Endocrinol. 2013 May 22;371(1-2):160-5. doi: 10.1016/j.mce.2012.12.005. Epub 2012 Dec 20.

3.

Gene therapy for adenosine deaminase-deficient severe combined immune deficiency: clinical comparison of retroviral vectors and treatment plans.

Candotti F, Shaw KL, Muul L, Carbonaro D, Sokolic R, Choi C, Schurman SH, Garabedian E, Kesserwan C, Jagadeesh GJ, Fu PY, Gschweng E, Cooper A, Tisdale JF, Weinberg KI, Crooks GM, Kapoor N, Shah A, Abdel-Azim H, Yu XJ, Smogorzewska M, Wayne AS, Rosenblatt HM, Davis CM, Hanson C, Rishi RG, Wang X, Gjertson D, Yang OO, Balamurugan A, Bauer G, Ireland JA, Engel BC, Podsakoff GM, Hershfield MS, Blaese RM, Parkman R, Kohn DB.

Blood. 2012 Nov 1;120(18):3635-46. doi: 10.1182/blood-2012-02-400937. Epub 2012 Sep 11.

4.

Gene therapy/bone marrow transplantation in ADA-deficient mice: roles of enzyme-replacement therapy and cytoreduction.

Carbonaro DA, Jin X, Wang X, Yu XJ, Rozengurt N, Kaufman ML, Wang X, Gjertson D, Zhou Y, Blackburn MR, Kohn DB.

Blood. 2012 Nov 1;120(18):3677-87. doi: 10.1182/blood-2012-02-408591. Epub 2012 Jul 25.

5.

Highly efficient large-scale lentiviral vector concentration by tandem tangential flow filtration.

Cooper AR, Patel S, Senadheera S, Plath K, Kohn DB, Hollis RP.

J Virol Methods. 2011 Oct;177(1):1-9. doi: 10.1016/j.jviromet.2011.06.019. Epub 2011 Jul 18.

6.

Ex vivo transduction and transplantation of bone marrow cells for liver gene delivery of alpha1-antitrypsin.

Li H, Lu Y, Witek RP, Chang LJ, Campbell-Thompson M, Jorgensen M, Petersen B, Song S.

Mol Ther. 2010 Aug;18(8):1553-8. doi: 10.1038/mt.2010.116. Epub 2010 Jun 15.

7.

Optimal promoter usage for lentiviral vector-mediated transduction of cultured central nervous system cells.

Li M, Husic N, Lin Y, Christensen H, Malik I, McIver S, LaPash Daniels CM, Harris DA, Kotzbauer PT, Goldberg MP, Snider BJ.

J Neurosci Methods. 2010 May 30;189(1):56-64. doi: 10.1016/j.jneumeth.2010.03.019. Epub 2010 Mar 27.

8.

Stable transgene expression in primitive human CD34+ hematopoietic stem/progenitor cells, using the Sleeping Beauty transposon system.

Sumiyoshi T, Holt NG, Hollis RP, Ge S, Cannon PM, Crooks GM, Kohn DB.

Hum Gene Ther. 2009 Dec;20(12):1607-26. doi: 10.1089/hum.2009.109.

9.

TRIM28 mediates primer binding site-targeted silencing of Lys1,2 tRNA-utilizing retroviruses in embryonic cells.

Wolf D, Hug K, Goff SP.

Proc Natl Acad Sci U S A. 2008 Aug 26;105(34):12521-6. doi: 10.1073/pnas.0805540105. Epub 2008 Aug 19.

10.

Host restriction factors blocking retroviral replication.

Wolf D, Goff SP.

Annu Rev Genet. 2008;42:143-63. doi: 10.1146/annurev.genet.42.110807.091704. Review.

11.

Development of lentiviral vectors with regulated respiratory epithelial expression in vivo.

Hendrickson B, Senadheera D, Mishra S, Bui KC, Wang X, Chan B, Petersen D, Pepper K, Lutzko C.

Am J Respir Cell Mol Biol. 2007 Oct;37(4):414-23. Epub 2007 Jun 15.

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